Evidence map›Paper›PMID 40491862›Full record

ArticleGynecologic oncology reports2025

Low mitotic count may affect the prognosis of uterine leiomyosarcoma: A report of two cases.

Christine Cho, Ciara Marshall, Erik Washburn, Edward Podczaski, Joel Sorosky, Shaina Bruce

Abstract readCase Reports
In one paragraph

Article in Gynecologic oncology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Christine ChoDepartment of Obstetrics and Gynecology at Penn State Health Hershey Medical Center, United States.
Ciara MarshallDepartment of Obstetrics and Gynecology at Penn State Health Hershey Medical Center, United States.
Erik WashburnDepartment of Pathology at Penn State Health Hershey Medical Center, United States.
Edward PodczaskiDivision of Gynecology Oncology at Penn State Health Hershey Medical Center, United States.
Joel SoroskyDivision of Gynecology Oncology at Penn State Health Hershey Medical Center, United States.
Shaina BruceDivision of Gynecology Oncology at Penn State Health Hershey Medical Center, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Uterine leiomyosarcoma (uLMS) is characterized by its aggressive nature, early metastatic potential, and poor clinical outcomes. Diagnosis of uLMS requires two out of the following three diagnostic criteria: marked cytologic atypia, 10 mitoses per 10 high power fields, tumor cell necrosis. This case series presents two cases of uLMS with a low mitotic rate and an indolent disease course, with excellent response to hormone therapies. Case 1: A 44-year-old female was diagnosed with uLMS following a supracervical hysterectomy in 2006. The primary tumor demonstrated tumor cell necrosis, cytologic atypic, and 6 mitoses per 10 HPF. Her 18-year disease course is notable for four debulking surgeries and multiple courses of hormonal therapy resulting in durable responses. Case 2: A 75-year-old female was diagnosed with smooth muscle tumor of uncertain malignant potential (STUMP) status post debulking surgery which was revised to leiomyosarcoma following lung biopsy confirmation of metastasis. The primary tumor and lung biopsy demonstrated tumor cell necrosis, cytologic atypia and 2 mitosis per 10 HPF. She demonstrated stable disease on letrozole for 11 months. Discussion: These cases demonstrate that uLMS with low mitotic activity may exhibit less aggressive behavior than typical high-grade sarcomas. Recognizing this distinction can guide prognostication and treatment selection.

Indexed as

Indolent diseaseLeiomyosarcomasNomograms for future use of uterine leiomyosarcoma classificationUterine sarcomas

Identifiers

PMID40491862
PMCPMC12148443

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